Variant report

Variant rs716387
Chromosome Location chr9:73900251-73900252
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:73896400-73900400 Weak transcription HepG2 liver
2 chr9:73900000-73900600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
3 chr9:73900000-73901400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr9:73900200-73900600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr9:73900200-73900600 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr9:73900200-73900600 Flanking Active TSS Liver Liver
7 chr9:73900200-73900600 Active TSS Brain Hippocampus Middle brain
8 chr9:73900200-73900600 Active TSS Brain Inferior Temporal Lobe brain
9 chr9:73900200-73900600 Active TSS Brain Substantia Nigra brain
10 chr9:73900200-73900600 Active TSS Pancreatic Islets Pancreatic Islet
11 chr9:73900200-73900600 Active TSS Osteobl bone
12 chr9:73900200-73900800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr9:73900200-73900800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr9:73900200-73900800 Enhancers iPS-18 Cell Line embryonic stem cell
15 chr9:73900200-73900800 Enhancers Aorta Aorta
16 chr9:73900200-73901400 Enhancers iPS-20b Cell Line embryonic stem cell
17 chr9:73900200-73901600 Enhancers HUES48 Cell Line embryonic stem cell

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